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I don't know if I'm getting better or just used to the pain.
Bipolar for all0 -
Trigeminal Neuraligia is experienced by many people and is also common for people with MS like me. There is a really useful association for sufferers including a forum at tna.org.uk0
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http://braintalkcommunities.org/forums/
is a site I use reasonably often. There are forums for pretty much every condition related to the brain or nervous system and quite a few other conditions besides.
There are people from a range of ages and nationalities and is good for sharing experiences, support and information.0 -
I am sorry I didnt realise I was doing wrong it looked like a good site for people like myself, I dont know how a site who is set up to help people could be spamming I do not understand, and I dont know how to remove my post, again I am sorry for trying to share my find and will not be posting again as this is one of my first posts on here I feel realy disheartened and upset at this.0
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I am sorry I didnt realise I was doing wrong it looked like a good site for people like myself, I dont know how a site who is set up to help people could be spamming I do not understand, and I dont know how to remove my post, again I am sorry for trying to share my find and will not be posting again as this is one of my first posts on here I feel realy disheartened and upset at this.
At the bottom of your post, there should be an edit button. Click on that and there's the option to delete your post.Sealed pot challenge #232. Gold stars from Sue-UU - :staradmin :staradmin £75.29 banked
50p saver #40 £20 banked
Virtual sealed pot #178 £80.250 -
Can I ask who you are to ask me to remove my post? are you part of the MSE team as I have not been abusive just tried to be of help to other users, so how can I be inconveniencing the abuse team, I used to love looking on these forums for help and suggestions on the days when I dont leave my home. a very upset user.0
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Hi All,
My father who has myositis have created a social media site for the physically disabled community called Bee Enabled .co.uk
The idea being to share information on living aids, holiday experiences, days out in fact anything to do with helping members with day to day living.
Please take alook and let us know your thoughts0 -
I am having a few problems finding wheelchair sports in Dorset. Let me give you some info. about me before you say anything.
I'm 45, I am not wheelchair bound, but have had numerous ops. on my legs (39 in total) including knee cap removals, but no replacements. My legs are wobbly and I want to play some serious sports in Poole preferably, but willing to travel a bit.
I want to do things like basketball or rugby, maybe even wheelchair races. I don't want to be stuck playing gentle sports as my GP calls it, because I am not that way inclined. I used to play many sports before my legs gave up on me, and listened to my GP and surgeons telling me to be careful and now I am not listening I want to play.
So, are there any sports clubs in Poole or Dorset that do serious sports like those mentioned?
:beer:0 -
Fibromyalgia Association FMA UK can be found at http://www.fibromyalgia-associationuk.org/ and http://www.fmauk.org/
The Forum can be found here: http://www.fibromyalgia-associationuk.org/phpBB3/index.php?sid=e5a3d66fc97be869b5c358e427d5bcf60 -
Hi, I also wanted to add a forum - Spokz People specialise in physical disability and they have a new free forum on disability, relationships and intimacy. Forum posts can be answered by members of the public and also by Spokz People's qualified counsellors and sex therapists. Type Spokz People into google and it will pop up.
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